Pilot Study of Remote Glucose Monitoring Among Pediatric Patients With Type 1 Diabetes

NCT ID: NCT04696640

Last Updated: 2022-06-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

39 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-03

Study Completion Date

2022-05-25

Brief Summary

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This project explores the feasibility and utility of remote glucose monitoring for a cohort of children and adolescents with type 1 diabetes (T1D) cared for at UC Davis Health (UCDH).

Detailed Description

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Conditions

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Type 1 Diabetes

Study Design

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Allocation Method

NA

Intervention Model

SEQUENTIAL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Remote Patient Monitoring

All participants who have successfully established remote data-sharing from their glucose monitors to the research team's Glooko account by conclusion of the one-month baseline period will advance to the six-month intervention period.

Group Type EXPERIMENTAL

Remote Patient Monitoring

Intervention Type BEHAVIORAL

Participants' glucose data will be monitored by the study team using population analytic reports. Participants who either have excessive hypoglycemia or hyperglycemia on these reports will be contacted by a pediatric endocrinologist (the principal investigator) to discuss any necessary adjustments to their home diabetes management plans. This intervention will be in addition to their usual care (regular visits at the UC Davis Pediatric Endocrinology clinic).

Interventions

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Remote Patient Monitoring

Participants' glucose data will be monitored by the study team using population analytic reports. Participants who either have excessive hypoglycemia or hyperglycemia on these reports will be contacted by a pediatric endocrinologist (the principal investigator) to discuss any necessary adjustments to their home diabetes management plans. This intervention will be in addition to their usual care (regular visits at the UC Davis Pediatric Endocrinology clinic).

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Diagnoses of type 1 diabetes with a duration of greater than or equal to 12 months
* Use of a continuous glucose monitor (CGM) for greater than or equal to 6 months
* Intention to continue receiving care at the UC Davis Health Pediatric Diabetes clinic.

Exclusion Criteria

* Patient's CGM cannot be uploaded to Glooko
Minimum Eligible Age

1 Year

Maximum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of California, Davis

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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University of California-Davis

Sacramento, California, United States

Site Status

Countries

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United States

References

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Crossen SS, Romero CC, Lewis C, Glaser NS. Remote glucose monitoring is feasible for patients and providers using a commercially available population health platform. Front Endocrinol (Lausanne). 2023 Feb 2;14:1063290. doi: 10.3389/fendo.2023.1063290. eCollection 2023.

Reference Type DERIVED
PMID: 36817610 (View on PubMed)

Related Links

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Other Identifiers

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1638182

Identifier Type: -

Identifier Source: org_study_id

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